(Q24799429)

English

Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications

scientific article

In more languages

Statements

scholarly article

0 references

1 reference

6 November 2020

Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications (English)

0 references

1 reference

6 November 2020

methylenetetrahydrofolate reductase

1 reference

6 November 2020

genetic polymorphism

1 reference

transcobalamins

1 reference

Henrik Zetterberg

1

0 references

language of work or name

0 references

publication date

17 February 2004

11 references

13 March 2019

19 June 2019

30 June 2019

3 August 2019

14 September 2019

28 September 2019

27 November 2019

28 November 2019

12 December 2019

13 December 2019

6 November 2020

Reproductive Biology and Endocrinology

12 references

14 February 2019

13 March 2019

19 June 2019

30 June 2019

3 August 2019

14 September 2019

28 September 2019

27 November 2019

28 November 2019

12 December 2019

13 December 2019

6 November 2020

2

0 references

1

0 references

7

0 references

Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

Impact of folic acid fortification of the US food supply on the occurrence of neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

The transcobalamin (TC) codon 259 genetic polymorphism influences holo-TC concentration in cerebrospinal fluid from patients with Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

7 April 2017

Fortification, supplementation, and nutrient balance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Teratogenic alleles and neurodevelopmental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Thrombophilic disorders and fetal loss: a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Homocysteine, folic acid and B-group vitamins in obstetrics and gynaecology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Hyperhomocysteinaemia and human reproduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Folate, homocysteine and neural tube defects: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Folic acid and human malformations: a summary and evaluation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Susceptibility to spina bifida; an association study of five candidate genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Health implications of Mediterranean diets in light of contemporary knowledge. 1. Plant foods and dairy products

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Neurological involvement in hereditary transcobalamin II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Vitamin deficiencies and neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 September 2017

Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

Increased frequency of genetic thrombophilia in women with complications of pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

Can terathanasia explain the protective effect of folic-acid supplementation on birth defects?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

Disruption of thymidylate synthesis and glycine-serine interconversion by L-methionine and L-homocystine in Raji cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

Hyperhomocysteinaemia and recurrent spontaneous abortion or abruptio placentae

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

30 May 2018

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Gene-gene interaction between fetal MTHFR 677C>T and transcobalamin 776C>G polymorphisms in human spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Antiphospholipid/antiprotein antibodies, hemostasis-related autoantibodies, and plasma homocysteine as risk factors for a first early pregnancy loss: a matched case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

The transcobalamin codon 259 polymorphism should be designated 776C>G, not 775G>C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Plasma homocysteine levels correlated to interactions between folate status and methylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Homocysteine is embryotoxic but does not cause neural tube defects in mouse embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

No association between the MTHFR A1298C and transcobalamin C776G genetic polymorphisms and hyperhomocysteinemia in thrombotic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Folic acid supplements during early pregnancy and likelihood of multiple births: a population-based cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

The transcobalamin codon 259 polymorphism influences the risk of human spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Plasma folate levels and risk of spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Importance of both folic acid and vitamin B12 in reduction of risk of vascular disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

MTRR and MTHFR polymorphism: link to Down syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Transcobalamin polymorphism and homocysteine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Use of multivitamins and folic acid in early pregnancy and multiple births in Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Postnatal screening for thrombophilia in women with severe pregnancy complications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Hyperhomocysteinemia and recurrent early pregnancy loss: a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Mutations in coagulation factors in women with unexplained late fetal loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Neural-tube defects and derangement of homocysteine metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=356929

28 November 2018

Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered folate and vitamin B12 metabolism in families with spina bifida offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

776C>G polymorphism of the transcobalamin II gene as a risk factor for spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Higher rate of multiple births after periconceptional vitamin supplementation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary habitual abortions are associated with high frequency of factor V Leiden mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C-->T mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neural-tube defects are associated with low concentrations of cobalamin (vitamin B12) in amniotic fluid

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent early pregnancy loss and genetic-related disturbances in folate and homocysteine metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk factor for unexplained recurrent early pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amniotic fluid homocysteine levels, 5,10-methylenetetrahydrafolate reductase genotypes, and neural tube closure sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Miscarriage and use of multi-vitamins or folic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of 677C-->T and 1298A-->C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent--the Nîmes Obstetricians and Haematologists Study5 (NOHA5)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14969589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1477-7827-2-7

0 references

Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1477-7827-2-7

PMC publication ID

0 references

PubMed publication ID

0 references

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24799429&oldid=2176917626"